EP0120548A2 - Improved process of making electrochemical electrodes and electrodes made thereby - Google Patents

Improved process of making electrochemical electrodes and electrodes made thereby Download PDF

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Publication number
EP0120548A2
EP0120548A2 EP84200460A EP84200460A EP0120548A2 EP 0120548 A2 EP0120548 A2 EP 0120548A2 EP 84200460 A EP84200460 A EP 84200460A EP 84200460 A EP84200460 A EP 84200460A EP 0120548 A2 EP0120548 A2 EP 0120548A2
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EP
European Patent Office
Prior art keywords
electrode
roll
layers
bonding
active
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
EP84200460A
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German (de)
French (fr)
Other versions
EP0120548B1 (en
EP0120548A3 (en
Inventor
Ronald Albert Howard
Paul Stephen Sirocky
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Union Carbide Corp
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Union Carbide Corp
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Filing date
Publication date
Application filed by Union Carbide Corp filed Critical Union Carbide Corp
Priority to AT84200460T priority Critical patent/ATE28535T1/en
Publication of EP0120548A2 publication Critical patent/EP0120548A2/en
Publication of EP0120548A3 publication Critical patent/EP0120548A3/en
Application granted granted Critical
Publication of EP0120548B1 publication Critical patent/EP0120548B1/en
Expired legal-status Critical Current

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    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00Electrodes
    • H01M4/86Inert electrodes with catalytic activity, e.g. for fuel cells
    • H01M4/88Processes of manufacture
    • H01M4/8878Treatment steps after deposition of the catalytic active composition or after shaping of the electrode being free-standing body
    • H01M4/8896Pressing, rolling, calendering
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00Electrodes
    • H01M4/86Inert electrodes with catalytic activity, e.g. for fuel cells
    • H01M4/8663Selection of inactive substances as ingredients for catalytic active masses, e.g. binders, fillers
    • H01M4/8668Binders
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00Electrodes
    • H01M4/86Inert electrodes with catalytic activity, e.g. for fuel cells
    • H01M4/8663Selection of inactive substances as ingredients for catalytic active masses, e.g. binders, fillers
    • H01M4/8673Electrically conductive fillers
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00Electrodes
    • H01M4/86Inert electrodes with catalytic activity, e.g. for fuel cells
    • H01M4/96Carbon-based electrodes
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E60/00Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/30Hydrogen technology
    • Y02E60/50Fuel cells

Definitions

  • the present invention is in the field of electrochemical cell electrodes. More specifically, the present invention is in the field of air-depolarized cathodes.
  • these cathodes usually consist of at least two layers: a current collector, which may be a wire mesh screen or a similar conductive framework, and an active layer wherein the desired electrochemical reaction takes place. Additional layers often include a wetproofing layer made with a high concentration of a hydrophobic material such as polytetrafluoroethylene or other suitable polymers.
  • the wetproofing layer may contain pore formers that are removed after processing to produce fine porosity in the layer as is taught in U.S. Patent 3,594,236.
  • the active layer as well as the wetproofing layer may contain pore formers as taught in U.S. Patent 4,370,284.
  • the layers of cathodes are normally pressed together between platens in a hydraulic press or they are rolled together in a roll mill.
  • both laminating methods have limitations.
  • For the pressing method extremely high tonnage presses are required and with this type of press, the uniformity of the pressing decreases because of elastic deflection of the equipment at high pressure.
  • the limitation of the roll bonding method is mainly in the uniformity of the layers being bonded. These layers will always have some variation in thickness or density. When long pieces of cathode are rolled with these variations, the layers will not lay in a straight line during rolling and the quality of the product will decrease.
  • the principal object of this invention is to provide an article of this character which combines simplicity, strength and durability in a high degree, together with inexpensiveness of construction.
  • Another important object is to provide a method of bonding the layers of a large cathode that can be adapted to production and which gives high quality, uniform permeability cathodes in which the layers are well bonded together.
  • the invention resides in a process for making an improved electrode by providing on a conductive current distributor layers of active and hydrophobic materials, uniting these materials together with a force the need not be greater than that sufficient to lock them together, and subsequently roll-bonding the resulting preformed assembly to form the finished electrode.
  • This two-stage process improves the bond strength between the layers and improves the uniformity of both the permeability and the bond strength of the layers.
  • the single figure in the drawing is a cross section of an electrode of the invention.
  • the electrode 10 includes a metal screen current distributor 12, a layer 14 of active material such as carbon, and hydrophobic layer 16 suitably of polymeric and hydrophobic material such as polytetrafluoroethylene (PTFE).
  • PTFE polytetrafluoroethylene
  • the metal screen or grid 12 may consist of various metals or alloys including nickel, silver, copper, stainless steel, iron, steel, and the like, and also the preceding metals plated with nickel or gold, silver, platinum, or other noble metals.
  • the active material 14 may consist of materials including carbon, activated carbon, catalysts, a pore former, and an appropriate binder.
  • the hydrophobic layer 16 may consist, in addition to that specified above, of polyethylene or polypropylene, or carbon mixed with such polymeric materials.
  • the two-stage laminating of these layers is accomplished by first laying up the screen, the active carbon layer, and the hydrophobic layer in a hydraulic press capable of applying a pressure of one-tenth to five tons per square inch based on the face area of the cathode.
  • the layers are pre-pressed and set into place with sufficient force only to lock all three layers together.
  • the pre-pressed cathode structure is then roll-bonded on a constant pressure rolling mill.
  • roll-bonding is meant the technique of passing the sheet-like prepressed stacked layers through the nip of a roll mill, which consists of counter-rotating rolls that are substantially cylindrical in shape and can exert line force pressures of from 35,7- 3570 kg/em.
  • the two-stage pressing and roll-bonding is altered by roll-bonding more than one time. This may be done with the intent to work the material gradually down so a specified disbond strength can be achieved. Thus, one obtains an average disbond strength of 0,49 kg/em2 by roll-bonding only once. Roll-bonding a second time will increase the average disbond strength to 1,05 kg/cm 2 .
  • cathodes having disbond strengths ranging from nearly zero to about 3 , 5 k g/ cm 2 can be made.
  • disbond strength is meant the hydraulic pressure required to separate the active layer from the current collector, wherein the hydraulic fluid is water and the test is conducted at room temperature.
  • Permeability is also influenced by the two stage process of this invention as increased rolling by using either higher pressure or multiple roll-bonding will decrease the permeability but will also produce the benefit of making the permeability more uniform across a large sheet. In practice, a compromise is struck between uniformity of properties and the level of the properties.
  • cathodes consisting of a silver plated nickel grid, finely divided activated carbon and PTFE were made by the prior art technology and by the process of this invention.
  • the pressed layer structure prepared according to the prior art showed variations in the disbond strength and permeability over a large range.
  • the two-stage process of the invention increases the average disbond strength between the layers and, more importantly, it also improves the uniformity over the entire structure.
  • Typical disbond strength variation in a pressed cathode shows a variation of 1,12 kg/cm 2 .
  • After roll bonding a variation of 5 psi is achieved.
  • This improved uniformity is also seen in the variation in permeability with variation in pressed cathodes of 8 ml/min/cm 2 at 15 cm of Hg, with individual values ranging from 5 to 21 ml/min/cm .
  • a variation of 5 ml/min/cm 2 at 15 cm of Hg, with individual values ranging from 12 to 17 ml/min/cm 2 is achieved after roll bonding.
  • dry nitrogen at an inlet pressure of 20 kPa above atmospheric pressure is passed through the sample and vented to atmospheric pressure.
  • cathodes having a measured permeability ranging from less than 1 ml/min/cm 2 to about 400 ml/min/cm 2 may be found useful, depending upon the end use.
  • An added unexpected benefit derived from the combination of processes is that of improved product uniformity as evidenced by greater uniformity in both disbond strength and porosity, i.e., gas flow rate through the finished electrode.

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  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Electrochemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Manufacturing & Machinery (AREA)
  • Battery Electrode And Active Subsutance (AREA)
  • Inert Electrodes (AREA)
  • Electrical Discharge Machining, Electrochemical Machining, And Combined Machining (AREA)
  • Electric Double-Layer Capacitors Or The Like (AREA)

Abstract

A process for making an improved electrode by providing on a conductive current distributor layers of active and hydrophobic materials, uniting these materials together with sufficient force to lock them together and subsequently roll-bonding the resulting preformed assembly to form the finished electrode.

Description

    FIELD OF THE INVENTION
  • The present invention is in the field of electrochemical cell electrodes. More specifically, the present invention is in the field of air-depolarized cathodes.
  • STATEMENT OF THE PRIOR ART
  • Considering only porous air-depolarized cathodes, these cathodes usually consist of at least two layers: a current collector, which may be a wire mesh screen or a similar conductive framework, and an active layer wherein the desired electrochemical reaction takes place. Additional layers often include a wetproofing layer made with a high concentration of a hydrophobic material such as polytetrafluoroethylene or other suitable polymers.
  • These layers are self bonding if enough pressure is applied by pressing or rolling. Rolling several layers together presents a variety of problems, most of which result in one's not being able to keep the layers in proper alignment. Pressing an electrode of large area has the disadvantage of requiring large presses capable of exerting many tons of force to achieve sufficient bonding. Also, the uniformity of the electrode layers and of the platen surfaces of the press under pressing conditions are important variables that are difficult to control.
  • The wetproofing layer may contain pore formers that are removed after processing to produce fine porosity in the layer as is taught in U.S. Patent 3,594,236. Similarly, the active layer as well as the wetproofing layer may contain pore formers as taught in U.S. Patent 4,370,284.
  • The layers of cathodes are normally pressed together between platens in a hydraulic press or they are rolled together in a roll mill. When large area cathodes are required for industrial applications, both laminating methods have limitations. For the pressing method, extremely high tonnage presses are required and with this type of press, the uniformity of the pressing decreases because of elastic deflection of the equipment at high pressure. The limitation of the roll bonding method is mainly in the uniformity of the layers being bonded. These layers will always have some variation in thickness or density. When long pieces of cathode are rolled with these variations, the layers will not lay in a straight line during rolling and the quality of the product will decrease.
  • OBJECTS AND SUMMARY OF THE INVENTION
  • The principal object of this invention is to provide an article of this character which combines simplicity, strength and durability in a high degree, together with inexpensiveness of construction.
  • Another important object is to provide a method of bonding the layers of a large cathode that can be adapted to production and which gives high quality, uniform permeability cathodes in which the layers are well bonded together.
  • Other objects of this invention will in part be obvious and in part hereinafter be pointed out.
  • . In summary, the invention resides in a process for making an improved electrode by providing on a conductive current distributor layers of active and hydrophobic materials, uniting these materials together with a force the need not be greater than that sufficient to lock them together, and subsequently roll-bonding the resulting preformed assembly to form the finished electrode. This two-stage process improves the bond strength between the layers and improves the uniformity of both the permeability and the bond strength of the layers.
  • BRIEF DESCRIPTION OF THE DRAWING
  • The single figure in the drawing is a cross section of an electrode of the invention.
  • DETAILED DESCRIPTION OF THE DRAWING
  • With reference to the drawing, there is shown an electrode constructed in accordance with the principles of the invention and designated generally by reference character 10. The electrode 10 includes a metal screen current distributor 12, a layer 14 of active material such as carbon, and hydrophobic layer 16 suitably of polymeric and hydrophobic material such as polytetrafluoroethylene (PTFE).
  • In the practice of the invention, the metal screen or grid 12 may consist of various metals or alloys including nickel, silver, copper, stainless steel, iron, steel, and the like, and also the preceding metals plated with nickel or gold, silver, platinum, or other noble metals.
  • The active material 14 may consist of materials including carbon, activated carbon, catalysts, a pore former, and an appropriate binder.
  • The hydrophobic layer 16 may consist, in addition to that specified above, of polyethylene or polypropylene, or carbon mixed with such polymeric materials.
  • In the process of the invention, the two-stage laminating of these layers is accomplished by first laying up the screen, the active carbon layer, and the hydrophobic layer in a hydraulic press capable of applying a pressure of one-tenth to five tons per square inch based on the face area of the cathode. The layers are pre-pressed and set into place with sufficient force only to lock all three layers together. The pre-pressed cathode structure is then roll-bonded on a constant pressure rolling mill. By "roll-bonding" is meant the technique of passing the sheet-like prepressed stacked layers through the nip of a roll mill, which consists of counter-rotating rolls that are substantially cylindrical in shape and can exert line force pressures of from 35,7- 3570 kg/em.
  • In a modification of the process of the invention, the two-stage pressing and roll-bonding is altered by roll-bonding more than one time. This may be done with the intent to work the material gradually down so a specified disbond strength can be achieved. Thus, one obtains an average disbond strength of 0,49 kg/em2 by roll-bonding only once. Roll-bonding a second time will increase the average disbond strength to 1,05 kg/cm2. In practice and depending upon the end use, cathodes having disbond strengths ranging from nearly zero to about 3,5 kg/cm 2 can be made. By "disbond strength" is meant the hydraulic pressure required to separate the active layer from the current collector, wherein the hydraulic fluid is water and the test is conducted at room temperature.
  • Permeability is also influenced by the two stage process of this invention as increased rolling by using either higher pressure or multiple roll-bonding will decrease the permeability but will also produce the benefit of making the permeability more uniform across a large sheet. In practice, a compromise is struck between uniformity of properties and the level of the properties.
  • In the present process, the use of constant gap rolls achieves a similar effect but with less uniformity than with constant pressure rolls.
  • The invention is further illustrated in a non-limited manner by the following examples.
  • EXAMPLES
  • In this example, a number of cathodes consisting of a silver plated nickel grid, finely divided activated carbon and PTFE were made by the prior art technology and by the process of this invention.
  • The pressed layer structure prepared according to the prior art showed variations in the disbond strength and permeability over a large range. The two-stage process of the invention increases the average disbond strength between the layers and, more importantly, it also improves the uniformity over the entire structure.
  • Typical disbond strength variation in a pressed cathode shows a variation of 1,12 kg/cm2. After roll bonding a variation of 5 psi is achieved. This improved uniformity is also seen in the variation in permeability with variation in pressed cathodes of 8 ml/min/cm2 at 15 cm of Hg, with individual values ranging from 5 to 21 ml/min/cm . A variation of 5 ml/min/cm2 at 15 cm of Hg, with individual values ranging from 12 to 17 ml/min/cm2, is achieved after roll bonding. In this permeability test, dry nitrogen at an inlet pressure of 20 kPa above atmospheric pressure is passed through the sample and vented to atmospheric pressure. The flow rate is measured and is divided by the superficial flow area to obtain the reported value. In practice, cathodes having a measured permeability ranging from less than 1 ml/min/cm2 to about 400 ml/min/cm2 may be found useful, depending upon the end use.
  • Analysis of the data obtained with the above samples showed that many of the problems experienced in the rolling operation are eliminated if the electrode is pressed before rolling. The product from such a combination of operations is different from that of only pressing in that the materials are more tightly bonded, as indicated by increased disbond strengths. Further, lower pressures can be used in the pressing operation to make a "preform" followed by a rolling operation that creates the high pressures required to tightly bond the layers to one another. Thus, an increase in cathode area need not create the need for a higher capacity press.
  • An added unexpected benefit derived from the combination of processes is that of improved product uniformity as evidenced by greater uniformity in both disbond strength and porosity, i.e., gas flow rate through the finished electrode.
  • The article of the invention has been thoroughly tested under actual use conditions and has been found to be completely successful for the accomplishment of the above-stated objects of the invention. It is believed that the operation and use of the invention hereinabove described will be evident to those skilled in the art to which it relates from a consideration of the foregoing.

Claims (8)

1. A process for making an electrode comprising providing on a conductive current distributor layers of active and hydrophobic materials;
uniting said materials and said distributor with sufficient pressure to lock them together; and
roll-bonding the resulting preformed assembly at least once to form the electrode.
2. The process of claim I wherein a pore former is selectively included in the active layer and/or the hydrophobic layer, said pore former being removed after roll-bonding operations are complete.
3. The process of claim 1 or 2 wherein said pressure used for said uniting ranges from about 14 to about 700 kg/cm2.
4. The process of claim 1, 2, or 3 wherein said preformed assembly is roll-bonded more than once.
5. An electrode made by the process of claim 1, 2, 3, or 4 and characterized by a disbond strength of about 0,35 to about 2,1 kg/cm2.
6. The electrode of claims 1, 2, 3, 4, or 5, having a current distributor formed of a material selected from the group consisting of nickel, silver, copper, stainless steel, iron, steel, and the preceding metals plated with nickel or gold, silver, platinum, or othernoble merals.
7. The electrode of claim 5 or 6 wherein said active materials comprise activated carbon and a PTFE binder.
8. The electrode of claim 5, 6, or 7 wherein said hydrophobic material is PTFE.
EP84200460A 1983-03-29 1984-03-28 Improved process of making electrochemical electrodes and electrodes made thereby Expired EP0120548B1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
AT84200460T ATE28535T1 (en) 1983-03-29 1984-03-28 METHOD OF MAKING ELECTROCHEMICAL ELECTRODES AND ELECTRODES MANUFACTURED THEREFORE.

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US06/480,619 US4529672A (en) 1983-03-29 1983-03-29 Process of making electrochemical electrodes and electrodes made thereby
US480619 1983-03-29

Publications (3)

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EP0120548A2 true EP0120548A2 (en) 1984-10-03
EP0120548A3 EP0120548A3 (en) 1985-12-18
EP0120548B1 EP0120548B1 (en) 1987-07-22

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EP84200460A Expired EP0120548B1 (en) 1983-03-29 1984-03-28 Improved process of making electrochemical electrodes and electrodes made thereby

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US (1) US4529672A (en)
EP (1) EP0120548B1 (en)
JP (1) JPS59184464A (en)
AT (1) ATE28535T1 (en)
AU (1) AU560217B2 (en)
CA (1) CA1221658A (en)
DE (1) DE3464986D1 (en)
ZA (1) ZA842307B (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0144002A2 (en) * 1983-11-28 1985-06-12 VARTA Batterie Aktiengesellschaft Porous gas electrode
DE3616684A1 (en) * 1986-05-16 1987-11-19 Behr Industrieanlagen SPRAYER FOR ELECTROSTATIC COATING OF OBJECTS
FR2611087A1 (en) * 1987-02-17 1988-08-19 Sanyo Electric Co ALKALINE BATTERY WITH NEGATIVE ELECTRODE TO CADMIUM
DE10327500A1 (en) * 2003-06-17 2005-01-20 W. C. Heraeus Gmbh & Co. Kg Process for the production of electrode structures and electrode structure and their use
US7332238B2 (en) 2002-09-06 2008-02-19 The Gillette Company Electrochemical cells and systems

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US4610938A (en) * 1985-07-24 1986-09-09 Electric Power Research Institute Acid fuel cell
DE3788671T2 (en) * 1986-03-24 1994-04-28 Grace W R & Co Cathodic electrode.
US4654281A (en) * 1986-03-24 1987-03-31 W. R. Grace & Co. Composite cathodic electrode
JPS63187574A (en) * 1987-01-29 1988-08-03 Japan Gore Tex Inc Fuel cell electrode-matrix monobloc forming and its manufacture
JPH0686463B2 (en) * 1988-07-01 1994-11-02 明治製菓株式会社 Novel cephem compound, its production method and antibacterial agent
US4925752A (en) * 1989-03-03 1990-05-15 Fauteux Denis G Solid state electrochemical cell having porous cathode current collector
JPH0491117U (en) * 1990-12-26 1992-08-07
US5478594A (en) * 1993-08-27 1995-12-26 Eveready Battery Company, Inc. Electrode structure for nickel metal hydride cells
US5916515A (en) * 1997-02-27 1999-06-29 Valence Technology, Inc. Two-stage lamination process
CN1085896C (en) * 1997-12-19 2002-05-29 王纪三 Electrode of charging battery and method and equipment for making electrode
JP2002030494A (en) * 2000-07-13 2002-01-31 Sumitomo Electric Ind Ltd Corrosion resistant electrically conductive member
DE10148599A1 (en) * 2001-10-02 2003-04-10 Bayer Ag Production of foil, used in production of gas diffusion electrodes for producing chlorine and caustic soda, involves rolling dry powder mixture of foil material while maintaining roll gap during rolling process
JP2009199963A (en) * 2008-02-25 2009-09-03 Fuji Heavy Ind Ltd Power storage device, electrode, manufacturing method for electrode, and management method

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FR2195849A1 (en) * 1972-08-14 1974-03-08 Studiecentrum V Or Sck Fuel cell electrode - with metal grid coated with two conducting catalyst-contg porous layers having different porosities
US4104197A (en) * 1975-12-17 1978-08-01 Licentia Patent-Verwaltungs-G.M.B.H. Method of making gas diffusion electrodes for electrochemical cells with acid electrolytes
GB2018501A (en) * 1978-03-20 1979-10-17 Varta Batterie Method of producing an air-depolarised electrode
EP0051440A1 (en) * 1980-10-31 1982-05-12 Eltech Systems Corporation Chlor-alkali cell with non-bleeding electrode

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US3594236A (en) * 1967-11-22 1971-07-20 Esb Inc Method for preparing an air breathing electrode
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Publication number Priority date Publication date Assignee Title
FR2195849A1 (en) * 1972-08-14 1974-03-08 Studiecentrum V Or Sck Fuel cell electrode - with metal grid coated with two conducting catalyst-contg porous layers having different porosities
US4104197A (en) * 1975-12-17 1978-08-01 Licentia Patent-Verwaltungs-G.M.B.H. Method of making gas diffusion electrodes for electrochemical cells with acid electrolytes
GB2018501A (en) * 1978-03-20 1979-10-17 Varta Batterie Method of producing an air-depolarised electrode
EP0051440A1 (en) * 1980-10-31 1982-05-12 Eltech Systems Corporation Chlor-alkali cell with non-bleeding electrode

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0144002A2 (en) * 1983-11-28 1985-06-12 VARTA Batterie Aktiengesellschaft Porous gas electrode
EP0144002A3 (en) * 1983-11-28 1986-12-17 Varta Batterie Aktiengesellschaft Porous gas electrode
DE3616684A1 (en) * 1986-05-16 1987-11-19 Behr Industrieanlagen SPRAYER FOR ELECTROSTATIC COATING OF OBJECTS
FR2611087A1 (en) * 1987-02-17 1988-08-19 Sanyo Electric Co ALKALINE BATTERY WITH NEGATIVE ELECTRODE TO CADMIUM
US7332238B2 (en) 2002-09-06 2008-02-19 The Gillette Company Electrochemical cells and systems
DE10327500A1 (en) * 2003-06-17 2005-01-20 W. C. Heraeus Gmbh & Co. Kg Process for the production of electrode structures and electrode structure and their use
DE10327500B4 (en) * 2003-06-17 2007-03-15 W.C. Heraeus Gmbh Process for the production of electrode structures and electrode structure and their use

Also Published As

Publication number Publication date
US4529672A (en) 1985-07-16
AU560217B2 (en) 1987-04-02
EP0120548B1 (en) 1987-07-22
ZA842307B (en) 1984-11-28
AU2625484A (en) 1984-10-04
CA1221658A (en) 1987-05-12
EP0120548A3 (en) 1985-12-18
DE3464986D1 (en) 1987-08-27
ATE28535T1 (en) 1987-08-15
JPS59184464A (en) 1984-10-19

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